Montelukast is a potent and selective adversary of the cysteinyl leukotriene receptor ( cysLT1 ) . It competitively antagonise cysLT1 receptor mediated bronchoconstriction, increased vascular permeableness and enlisting of eosinophils. Leukotriene receptor inhibitors are compounds of a new pharmacological category for asthma direction and their find had made a signii¬?cant impact on intervention schemes of asthma direction.

Montelukast is available in salt signifier as montelukast Sodium and described chemically as 1- [ ( { ( R ) -m- [ ( E ) -2- ( 7-chloro-2-quinolyl ) -vinyl ] -I±- [ o- ( 1-hydroxy-1-methylethyl ) phenethyl ] -ben-zyl } thio ) methyl ] cyclopropaneacetate.

Montelukast was discovered in 1990 and is used in the direction of chronic asthma, allergic coryza, and as prophylaxis for exercise-induced asthma. It is available as 5mg, 10mg movie coated and cuttable tablet and 4mg unwritten granules signifier.

Cysteinyl Leukotriene receptor go-betweens:

Leukotrienes were antecedently called as slow responding substance of Anaphylaxis ‘ or SRS-A. These are ini¬‚ammatory substances released by mast cells during the immediate response to inhaled allergen. Leukotriens are derived from arachidonic acid which is a precursor of prostaglandins ( Wasserman 1988 ; Wenzel 1997 ) . Leukotrienes can be divided into two households. One is leukotriene B4 which acts chiefly in conditions in which ini¬‚ammation is produced by neutrophils such as ini¬‚ammatory intestine disease, cystic i¬?brosis, and psoriasis. The other group is of ( C4, D4, E4 ) , called cysteinyl leukotrienes, bind to extremely selective leukotriens receptors to bring on eosinophil- and mast cell- induced bronchoconstriction and ini¬‚ammation that cause asthma ( Davis 1997 ) .Leukotrine 4 ( LTD 4 ) was found to be 1000 times more powerful than histamine in the contraction of smooth musculuss.

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Drugs that can interfere with the production of leukotriens and their binding to receptor have been designed. Leukotriene synthesis inhibitors ( e.g. zileuton ) , inhibit the enzyme 5-lipoxygenase and therefore barricade many leukotrienes production ( e.g. B4, C4, D4, and E4 ) ( Georgitis 1999 ) . Leukotriene receptor adversaries ( e.g. montelukast, zai¬?rlukast, pranlukast ) block leukotriene D4 ( LTD4 ) receptors ( Georgitis 1999 ) . Both leukotriene modii¬?ers types are administered orally as tablets.

Discovery of montelukast:

In late 1930 ‘s, Felldberg and Kalaway, two Australian scientist, observed the release of a substance from the lungs of guinea hogs, when the treated it with antigen. They found that this substance caused the contraction of smooth musculuss and they named it ‘slow responding substance of Anaphylaxis ‘ or SRS-A. The manner of contraction was different from histamine as this substance caused slow and sustained contraction ( histamine causes a rapid and reversible contraction ) . It was hard to depict it structural features, nevertheless, it was thought to be produce from mast cells and poly morphonuclear leucocytes. Later surveies showed that rhinal polyps and human lungs were able to bring forth this substance and it was the ground of human asthma.

A figure of pharmaceutical companies started to look into SRS-A, to develop a theray for Asthma intervention. In 1970 ‘s, research workers working at Merck frosst centre of curative research, used SRS-A to test its lead construction by working on Guinea hog ileum. At that clip, workers in England discovered foremost putative adversary of SRS-A, which was named FPL-55712.

After a long period research, Bengt Samuelsson of the Karolinska institute in 1979, proposed the construction of SRS-A which he named Leukotriene C. As consequence of important work it was proposed that SRS-A was the mixture of Leukotrienes C4, D4 and E4 ( LTC4, LTD4 & A ; LTE4 ) , which are different from each other on the footing of cystine incorporating prptide attached at C 6 place.

Biosynthesis of cysteinylleukotriene

Further studied showed that LTD4 was the outstanding character nowadays in SRS-A and responsible for bronchoconstriction and alterations in vascular permeableness. These surveies lead to the hypothesis that the blocker of leukotriene 4 might be utile in intervention of asthma. In 1980 ‘s, a big figure of Leukotriene adversaries were discovered by Lilly and Merck, with better authority than FPL-57712. But still these were non as potent to order for asthma intervention and it led to farther research. Majority of the compounds were non safe in regard to liver and kidney profile on treated animate beings. Research workers were met letdown many times and at last in 1990 they were successful able to detect a safe drug named Montelukast ( MK-0476 ) .

Mechanism of action:

Montelukast is a selective, reversible leukotriene receptor adversary. Leukotrienes were first

discovered in the 1930 ‘s as powerful go-betweens of redness and given the name slow-reacting

substance of anaphylaxis. Bronchoconstriction, increased mucose formation, and increased

vascular permeableness with edema formation are all possible mechanisms of airflow obstructor

secondary to leukotrienes. The cysteinyl leukotriene ( LTC4, LTD4, and LTE4 ) are merchandises of arachadonic acid metamorphosis which are released by mast cells, monocytes, eosinophils, and basophils. Surveies have shown LTD4 to be 140 to 6,000 times more powerful than histamine as a bronchoconstrictor. Montelukast binds with high affinity to the LTD4 receptor, suppressing bronchoconstriction. In clinical tests, montelukast has been found to suppress bronchoconstriction at doses runing from 5 to 250 milligrams, when administered four hours prior to a nebulized LTD4 challenge. , , , ,

Clinical Pharmacology of montelukast:

Montelukast has rapid oncoming of action, and produce betterment even after the first twenty-four hours of intervention. Montelukast besides produces good effects as if given with inhaled corticoids.


Montelukast is quickly captive following unwritten disposal, making extremum degrees 2 to 2.5 hours after disposal of the 5 milligram tablet and 2 to 4 hours after disposal of the 10 milligram tablet. , , . Bioavailability varies between the two tablet strengths. The 10 milligram tablet is about 64 % bioavailable, irrespective of whether it is administered with nutrient. The 5 milligram tablet is 73 % bioavailable in the fasting province, but bioavailability diminutions to 63 % when it is taken with nutrient. Montelukast is 100 % protein bound. , ,

Montelukast undergoes extended metamorphosis in the liver by the cytochrome P450 enzyme system, specifically CYP3A4 and CYP2C9, and is excreted into the bile. , , The average plasma half life of the drug is 2.7 to 5.5 hours. Patients with mild to chair hepatic disfunction and grounds of cirrhosis have been shown to hold a lessening in metamorphosis and a resulting addition in AUC of 40 % with a drawn-out riddance half life. Despite these effects, dose accommodation has non been required for patients with liver disease. Dose accommodations are besides non necessary for patients with nephritic disfunction.

Dosing recommendations:

Montelukast is presently available as Singulair, manufactured by Merck. It is available as a 5 milligram cuttable tablet and a 10 milligram film-coated tablet. Presently, there is no parenteral signifier of the drug. The recommended dose for kids 6 to 14 old ages of age is one 5 milligram cuttable tablet daily in the eventide. For patients & gt ; 15 old ages of age, the usual dose is 10 mg daily in the eventide. The maximal day-to-day dosage of montelukast is 10 milligram, although doses every bit high as 250 milligrams have been found to be safe in clinical tests. Higher doses, nevertheless, have non been found to better efficacy. ,

Patients should be advised to take montelukast even if they are symptomless and non to alter the dosage without the recommendation of a doctor. Patients should besides be reminded that this agent is non to be used for an acute asthma onslaught. Although montelukast maps as an anti- inflammatory, it should non be suddenly substituted for inhaled corticoids. Phenylketonurics should non have the 5 milligram cuttable tablets, as that dose signifier contains phenylalanine.

Curative Applications:

Montelukast is indicated for the prophylaxis and chronic intervention of asthma in patients greater

than six old ages of age. Unlike the other leukotriene adversaries, zafirlukast and zileuton,

montelukast is approved by the Food and Drug Administration ( FDA ) for usage in immature kids.

Blessing for exercise-induced asthma has non yet been established. , . Montelukast can be administered orally one time a twenty-four hours and increase the conformity of wheezing patients. It has efficient consequence against allergens, brochoconstrition and exercising induced asthma. No serious adverse and side effects of montelukast have been reported yet. It is the lone leukotriene receptor anatagonist which is approved by the Food and drug disposal to be administered in kids of 2 to 12 old ages of age.

The chief curative applications of montelukast are as follows:


Bronchiolitiss due to RSV infection frequently change to post bronchiolitic reactive air passages disease, which produce asthma-like wheeze and some other symptoms of asthma. In a pilot survey, montelukast 5 milligrams orally was given daily for 4 hebdomads to babies who were admitted in infirmary for moderate to severe bronchiolitis. It was observed that the symptoms of asthma and daytime cough was reduced, and more conformity was seen compared with placebo.

The good effects of montelukast over placebo were evident after 2 hebdomads of intervention. Although the safety and efficaciousness of such intervention should be to be decently established.

Efficacy in Asthma:

Asthma is the most frequent acknowledging diagnosing for kids and a prima cause of chronic

unwellness. For many old ages, bronchoconstriction was thought to be the primary mechanism of this

disease. However, chronic redness has now been recognized as the major cause of asthma exacerbations. , . Current recommendations for the intervention of chronic asthma now include

consistent intervention of redness as a primary end. Research is being focused on developing

drugs to suppress inflammatory go-betweens. Montelukast is among the new agents targeted at

cut downing redness in hopes of relieving asthma symptoms.

Montelukast produced betterments in comparing to placebo in chronic and exercise-induced asthma in both grownups, and children. , , . In a systematic surveies of montelukast in grownups and kids comparing leukotriene receptor antagonists with inhaled corticoids for the intervention of mild to chair asthma. In half of the surveies, montelukast was used, found to be less effectual in pull offing asthma control. A more recent survey in kids produced a similar decision, but another survey of 12 months in kids with mild relentless asthma, showed that montelukast was non inferior to an inhaled corticoid ( fluticasone ) .

It was observed that intervention with leukotriene receptor adversary like Montelukast led to 10-15 % betterment in baseline lung map of asthma patients even after the first dosage administered. The efficacious consequences of montelukast were varied with intervention regimen and the damage in lung map of patient. However, montelukast caused 10-15 % betterment in lung map even in presence and absence of linear therapy of inhaled corticoids. It was besides observed in 6-13 hebdomad test that no tolerance against montelukast was developed in the patient. Addition of montelukast to an inhaled corticoid has significantly improved asthma control in kids, and grownups with mild to chair asthma.

Improvement in a assortment of symptoms like entire asthma symptoms besides affecting dark clip rousing and forenoon clip asthma symptoms were seen every bit good as inhaled I?2 adversary usage was decreased. In 3 months surveies of montelukast, symptoms betterment was besides seen. A peorocol was designed to analyze montelukast in combination with inhaled steroids. In the beginning high dosage of steroids was given and decrease in the dosage of steroids with montelukast or placebo was observed. The decrease in the dosage with montelukast was higher than with placebo. In 2003, a 16 hebdomad randomized, dual blind, controlled survey was designed and conducted on 639 patients to analyze the consequence of montelukast in attendant therapy of inhaled budesonide. It was concluded that the patients with persistant asthma symptoms and mild airway obstructor in malice of budesonide intervention, attendant intervention with montelukast was more important in bettering asthma. Montelukast is non recommended in acute asthma, nevertheless an endovenous signifier of montelukast is under probe for the intervention of terrible ague asthma. ,


Montelukast has been used, with some success, in systemic mastocytosis intervention in babies.


Other of import utilizations of montelukast involves its usage in seasonal allergic reaction coryza. Other of import utilizations of montelukast involves its usage in seasonal allergic reaction coryza. Allergic coryza is a world-wide wellness job that generates an of import health care load in footings of outpatient visits by grownups, kids and striplings. Harmonizing to the recent Alergologica 2005 survey, conducted by 300 allergologists in a sum of 4500 new patients, coryza or rhinoconjunctivitis represents the chief cause of audience among 55.5 % of all patients seen in Spanish allergology clinics. Placebo-controlled surveies have shown that it is effectual in the remedy of symptoms in both seasonal allergic coryza, , and perennial allergic coryza. A meta-analysis of leukotriene adversaries chiefly montelukast was done for the direction of allergic coryza. It was concluded that leukotriene adversaries were more effectual modestly than placebo and produced similar efficaciousness to antihistamines, and led to reducie nasal symptoms and improved rhinoconjunctivitis. However, even in combination with antihistamines, they are less effectual than corticodteroids. A later systematic reappraisal, in which different surveies of allergic coryza utilizing a combination of montelukast and an antihistamine were done. The consequences were comparable with intranasal corticoids. Besides, usage of montelukast in some patients with both allergic coryza and asthma, resulted in important betterments as compared with placebo.

Administration in kids.

Asthma by and large begins and has its greatest prevalence in kids younger than 5 old ages old. This age group frequently presents with intermittent symptoms ( i.e. , long symptomless periods inter-

rupted by episodes of asthma by and large in association with the common cold ) . The episodic nature of this type of asthma may be due to greater variableness of asthma in immature kids, under- coverage of symptoms because of trust on second-hand care-giver study, increased susceptibleness of respiratory infections, or decreased effectivity of current accountant intervention in the younger age group. A survey was conducted on 2-5 cryings of age kids to see effectivity of montelukast in this age group. It was observed Montelukast efficaciously reduced asthma aggravations in 2- to 5-year-old patients with intermittent asthma over 12 months of intervention and was by and large good tolerated.

Even with the recent blessing of montelukast by the FDA, clinical experience is still really limited. Merely one large-scale survey has been published to day of the month in kids with chronic asthma. Montelukast Na is available as unwritten granules and cuttable tablets for usage in kids. Oral granules are largely used and suited for babies as they can be given direct orally or assorted with a little sum of soft nutrient including juices. Oral doses are licensed for the direction of chronic asthma and every bit good as prophylaxis for exercise-induced asthma, are as follows:

aˆ? 6 months to 5 old ages, 4 mg daily taken in the eventide

aˆ? 6 to 14 old ages, 5 mg daily taken in the eventide

aˆ? 15 old ages and over, utilize the grownup dosage, 10mg of montelukast in eventide.

Montelukast is besides licensed for usage in allergic coryza and the above doses can be given in seasonal allergic coryza and perennial allergic coryza.

Cystic fibrosis.

In cystic fibrosis, patient experience bronchial hyper reactivity similar to that seen in asthma. Aspergillus as an antigen in organic structure stimulate leukotriens synthesis and T assistant cell redness and lead to cystic fibrosis. Leukotrienes receptor adversaries are proved to be good in intervention of cystic fibrosis.

In 2002, a little survey was conducted in kids enduring from cystic fibrosis and it was found that montelukast play an of import function in decrease of eosinophilic redness. Another survey, reported that lung map was improved, coughing and wheezing besides reduced. It was concluded that montelukast may bring forth mensurable anti-inflammatory activity in patients with cystic fibrosis. In a little group survey of grownup patients with cystic fibrosis, montelukast showed to better symptoms, in peculiar exercising tolerance and peak expiratory flow rates. A survey on pharmacokinetics of montelukast in cystic fibrosis showed that there is no demand of dose accommodation in patients with cystic fibrosis to achive same plasma concentration as is achieved in asthma. However, rhe effectivity of this concentration in both patients ( enduring from asthma and cystic fibrosis ) is unknown.

Sleep-disordered external respiration.

Montelukast administered with an intranasal corticoid is been reported to be good in a survey conducted in kids with residuary sleep-disordered external respiration after adenoidectomy and tonsillectomy.

Graft-versus-host disease.

A pilot survey was conducted in chronic graft-versus-host disease ( GVHD ) after allogeneic hematopoietic root cell organ transplant, in 15 of 19 individuals betterment was observed by adding montelukast in their standard immunosuppressive regimens. It was besides seen that in 4 patients marks of chronic GVHD were cured, 2 patients showed important betterment, and 9 patients showed moderate betterment.


One of the suspected inauspicious consequence of montelukast usage is urticaria. A survey was conduceted to look into usage of montelukast in the intervention of urtication and it produced variable consequences. In another survey, montelukast was used with antihistamine desloratadine for the intervention of delayed force per unit area urtication. It was reported to be more effectual than placebo when used in combinition.


From early clinical surveies it was reported that montelukast can be indicated for the intervention of eczema, , nevertheless there is demand of more work on it as more recent surveies are failed to demo any betterment in montelukast therapy compared with placebo. ,

Allergic pinkeye:

Recent survey on montelukast have done for its usage in allergic pinkeye and it was concluded that topical optic montelukast can be a possible curative drug with a new path of disposal that can be used for intervention of allergic pinkeye.

Gastrointestinal upsets.

Eosinophilic oesophagitis is rare status and affect eaosinophilic infiltration of gorge and besides do intermittent painful dysphagia. Brnifits of montelukast are reported by the patients enduring from with eosinophilic oesophagitis. In a systemic reappraisal of drugs recommended for diagnosing and intervention of eosinophilic oesophagitis it was seen that Leukotiens receptor adversaries at high doses induce sympothomeic alleviation. However, no betterment in histology was observed and current literature do non back up its usage in eosinophilic oesophagitis intervention.

Adverse effects & A ; Precautions:

Montelukast appears to be good tolerated. In clinical tests, the most common inauspicious consequence

reported was concern, happening in about 18 % of patients. Rash, indigestion, giddiness,

and abdominal hurting were all reported in less than 2 % of patients. Elevated liver aminotransferases

have been reported with montelukast usage, but non at a greater incidence than with placebo. A

little per centum of paediatric patients have experienced diarrhoea, sinusitis, and otitis media

during montelukast clinical tests. , .FDA ( Food and drug disposal ) investigated mood/ behaviour altering associated with montelukast in March 2008, other station selling inauspicious reactions were besides reported in some patients affecting depression, shudders, anxiety and suicidality.

Other inauspicious drug reactions associated with montelukast involve

Hepatic damage.

Montelukast is eliminated by hepatic metamorphosis. Although inauspicious effects on the liver of patients having montelukast are observed but still is non considered to be contraindicated in hepatic damage, and no dose accommodation is required in hepatic damage.

Clinical tests on Leukotrienes receptor adversaries affecting Zafrilukast and ziluton, , showed that they induce hepatitis and hepatic failure within 13 months or more, while tests on montelukast showed that it non do liver toxicity. Discontinuing montelukast usage lead to standardization of liver maps. It is recommend that liver map should be tested within 4 hebdomads of induction of therapy with any leukotriene modii¬?er and that proving must be repeated at regular intervals of at 3, 6, and 12 months.

Churg-Strauss syndrome.

It is a systemic little vas vasculitis affecting tegument, lungs, bosom, GI piece of land and peripheral nervousnesss. The aetiology of Churg-Strauss syndrome is unknown. However, it is reported that in rare instances it is associated with the usage of leukotriene receptor adversaries ( LRA ) such as montelukast. , , , , , . Relapse was observed in a patient with Churg syndrome who was in complete remittal when montelukast therapy was started.

Pregnancy and Lactation

Montelukast is classified as gestation class B. The drug has been shown to traverse the placenta of pregnant rats and coneies, but at that place have been no studies of its usage in pregnant adult females. Montelukast is besides known to be excreted into breastmilk, but merely limited information is available on the significance of this determination. Caution should be used prior to originating montelukast therapy in nursing mothers. ,


Cytochrome P450 inducers: Caution are recommended when montelukast is administerd with powerful inducers of the cytochrome P450 isoenzyme CYP3A4 such as Phenobarbital, diphenylhydantoin, valproate or rifampicin.

Corticosteroids. When montelukast and Orasone was administered concomitantly, they produced peripheral hydrops in a patient.

Phenobarbital. Changes in pharmacokinetic parametric quantities were observed in 14 healthy subjecrs taking phenobarbital 100 mg daily for 14 yearss, after administrating individual unwritten dosage of montelukast 10mg. Peak serum concentrations were reduced by 20 % and country under the serum concentration-time curve was besides reduced by 38 % . However, these consequences did non take to dose accommodation of montelukast when given with sodium thiopental.


The intervention of chronic asthma has seen many alterations in the past 15 old ages. The National

Institute of Health ‘s current guidelines for the diagnosing and direction of asthma recommend

day-to-day anti-inflammatory therapy as the most effectual method to command chronic asthma.

Leukotrienes have been shown to be go-betweens in the inflammatory procedure and first-class marks

for therapy aimed at cut downing chronic symptoms. Montelukast is safe to administrate in kids from six months to onwards, nevertheless, dose accommodation is necessary. Montelukast can forestall or modify more relentless asthma that has been associated with RSV. It besides proved to me most effectual in attendant therapy with cortico steroids. Overall, it is a safest drug with good tolerance and broad spectrum of indicants.


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